For our client Merck based in Aubonne, we are looking for a QA Engineering Expert for a duration of 9 months (until 31.12.2024).
Your role:
Ensure that equipment & automated systems implemented are in accordance with internal procedures and current guidelines/regulations (including procedures related to change, risk and deviation management)
Support Equipment and Automated Systems deviation management.
Support, review and approve change control proposal (CCP) as QA engineering for projects
Participate to risk assessments
Review and approve quality documents (design documents, validation plans & summary reports, procedures, protocols, data reviews, reports and procedural documents)
Ensure that validation, calibration and preventive maintenance programs are in place and are respected
Routine activities:
Review and approve quality documents (operational documents, procedures, forms, intervention report for automation activities) for equipment and automated systems activities
Ensure support for deviations related to equipment and automated systems including QA assessment, investigation and CAPA review / approval and closure
Ensure that periodical technical interventions programs are in place and respected.
Participate to annual reviews as required.
Ensure QA activities in SAP-PM system: equipment/system and maintenance plans creation /modification/removal
Support department to guarantee that equipment and automated systems procedures and forms are understandable and easy to complete and review.
Participate to seminars and training sessions on equipment and automated systems qualifications best practices to maintain "state-of-the-art" in-house expertise.
Ensure backup of the QA engineer for project and routine activities
For our client Merck based in Aubonne, we are looking for a QA Engineering Expert for a duration of 9 months (until 31.12.2024).
Your role:
Ensure that equipment & automated systems implemented are in accordance with internal procedures and current guidelines/regulations (including procedures related to change, risk and deviation management)
Support Equipment and Automated Systems deviation management.
Support, review and approve change control proposal (CCP) as QA engineering for projects
Participate to risk assessments
Review and approve quality documents (design documents, validation plans & summary reports, procedures, protocols, data reviews, reports and procedural documents)
Ensure that validation, calibration and preventive maintenance programs are in place and are respected
Routine activities:
Review and approve quality documents (operational documents, procedures, forms, intervention report for automation activities) for equipment and automated systems activities
Ensure support for deviations related to equipment and automated systems including QA assessment, investigation and CAPA review / approval and closure
Ensure that periodical technical interventions programs are in place and respected.
Participate to annual reviews as required.
Ensure QA activities in SAP-PM system: equipment/system and maintenance plans creation /modification/removal
Support department to guarantee that equipment and automated systems procedures and forms are understandable and easy to complete and review.
Participate to seminars and training sessions on equipment and automated systems qualifications best practices to maintain "state-of-the-art" in-house expertise.
Ensure backup of the QA engineer for project and routine activities
Découvre comment se déroule la procédure de candidature et comment nous pouvons t'aider à trouver un emploi.
1 de 8
postuler avec randstad.
Postuler avec nous, c'est facile. Nous examinerons ta candidature et verrons si tu corresponds au poste et à l'entreprise.
2 de 8
nous te contacterons.
Notre consultant t'appellera au moment qui te convient pour discuter de ta candidature et de tes aspirations professionnelles.
3 de 8
ton inscription.
Si tu n'as jamais travaillé avec nous auparavant, nous aurons besoin d'informations de base supplémentaires pour confirmer ton éligibilité à travailler en Suisse.
4 de 8
vérification des références et des antécédents.
Ensuite, nous devrons simplement vérifier quelques éléments – nous effectuerons les contrôles de conformité appropriés et te tiendrons informé.
5 de 8
L'emploi parfait pour toi.
Notre équipe d'experts organisera un entretien pour le poste pour lequel tu as postulé ou, si elle pense qu'il existe une meilleure opportunité, elle te proposera également des options alternatives.
6 de 8
Ton entretien.
Nous veillerons à ce que tu sois parfaitement préparé avant ton entretien et que tu saches exactement à quoi t'attendre – bonne chance!
7 de 8
Commence ton nouvel emploi.
Félicitations, tu es prêt à commencer ton nouvel emploi. L'équipe veillera à ce que tu sois parfaitement préparé pour ton premier jour.
8 de 8
soutien continu.
Après avoir commencé ta nouvelle mission, nous te contacterons pour avoir de tes nouvelles et t'apporter notre soutien dans ton nouveau rôle.
Within the scope of a challenging, ambitious and future-oriented project driven by a dynamic team in an inspiring environment, we look for a QA laboratory equipment/system specialist.Your Role :· Define the laboratory equipment/systems quality strategy including data integrity aspects· Review and approval of GxP documents, including URS, traceability matrix, risk assessments, systems drawings, procedures, qualification documents…· Collabo
Within the scope of a challenging, ambitious and future-oriented project driven by a dynamic team in an inspiring environment, we look for a QA laboratory equipment/system specialist.Your Role :· Define the laboratory equipment/systems quality strategy including data integrity aspects· Review and approval of GxP documents, including URS, traceability matrix, risk assessments, systems drawings, procedures, qualification documents…· Collabo
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